Visitor Monitoring Drug History: ILOSONE
 
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Label and Approval History

Drug Name: ILOSONE
FDA Application No: (NDA) 050010
Active Ingredient(s): ERYTHROMYCIN ESTOLATE
Company: LILLY
 
Label History
 
Labels are not available on this site for ILOSONE, (NDA) 050010
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/16/1998 024Manufacturing Change or Addition  
4/24/1997 022Labeling Revision  
10/28/1993 019Labeling Revision  
4/18/1994 018Control Supplement  
8/10/1992 016Labeling Revision  
8/22/1991 014Control Supplement  
4/3/1992 012Labeling Revision  
4/16/1990 009Labeling Revision  
1/7/1991 008Labeling Revision  
12/10/1990 007Labeling Revision  
12/10/1990 006Labeling Revision  
4/10/1990 003Chemistry Generic  
4/13/1967 000Approval  
 
Therapeutic Equivalents
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